Computational investigation of Rh-catalyzed three-component arylamidation of alkenes: mechanism, regioselectivity, and enantioselectivity

The Rh-catalyzed three-component arylamidation of allylic sulfides was studied computationally to explore the mechanism, regioselectivity, and enantioselectivity.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-11-04
DOI
https://doi.org/10.1039/d5qo00998g
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.87
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article

Computational investigation of Rh-catalyzed three-component arylamidation of alkenes: mechanism, regioselectivity, and enantioselectivity

2 citations
Organic Chemistry Frontiers
Catalytic C–H Functionalization Methods
1.87
article

Computational investigation of Rh-catalyzed three-component arylamidation of alkenes: mechanism, regioselectivity, and enantioselectivity

article en
2 citations

Abstract

The Rh-catalyzed three-component arylamidation of allylic sulfides was studied computationally to explore the mechanism, regioselectivity, and enantioselectivity.

Organic Chemistry FrontiersVol. 13(2)
Guangdong Pharmaceutical University (CN)
Openalex Percentile: Top 13%
Catalytic C–H Functionalization Methods
1.87
DOISourceOpenAlex
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Computational investigation of Rh-catalyzed three-component arylamidation of alkenes: mechanism, regioselectivity, and enantioselectivity · Organic Chemistry Frontiers (2025) | TGRS Research Map | TGRS